JPS6116415B2 - - Google Patents

Info

Publication number
JPS6116415B2
JPS6116415B2 JP57073947A JP7394782A JPS6116415B2 JP S6116415 B2 JPS6116415 B2 JP S6116415B2 JP 57073947 A JP57073947 A JP 57073947A JP 7394782 A JP7394782 A JP 7394782A JP S6116415 B2 JPS6116415 B2 JP S6116415B2
Authority
JP
Japan
Prior art keywords
graphite
outer shell
chromium
less
cast iron
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP57073947A
Other languages
Japanese (ja)
Other versions
JPS58193343A (en
Inventor
Yoshihiro Nakagawa
Takashi Hashimoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kubota Corp
Original Assignee
Kubota Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kubota Corp filed Critical Kubota Corp
Priority to JP7394782A priority Critical patent/JPS58193343A/en
Publication of JPS58193343A publication Critical patent/JPS58193343A/en
Publication of JPS6116415B2 publication Critical patent/JPS6116415B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は外殻高クロム材質中に黒鉛を晶出せし
めた複合高クロムロールに関する。 高クロムロールは冶金学的にはその基地組走織
中に微細なクロム炭化物を含んで成立しており、
耐摩耗性に優れるのが特長であるが、反面熱伝導
率が低く、同一圧延条件で熱間圧延に使用した場
合、他の熱伝導率の良いロールよりも圧延材と接
する胴最表面の温度上昇が大きいのが難点であ
る。これはロール胴表面の温度差に改因してロー
ルの耐肌荒性、耐摩耗性、耐クラツク性に悪影響
を及ぼすためである。 この欠点を改良する一つの方法として、可能な
限りクロムを少なくする方策も案出されるが、炭
素含有量との関係でカーバイドが減少し、高クロ
ムロール本来の優れた耐摩耗性を維持できなくな
るため限度がある。 ところで、高クロムロールについては組織中に
硬い炭化物のみを有し、黒鉛は全く晶出しないと
するのが技術通念であり、又実際黒鉛を有するも
のは従来全く見当らないものであるが、一方本発
明者の研究によると、もしその組成中に黒鉛を晶
出することが可能ならば、高クロムロールの熱伝
導性を改善することができ、これによつて上記圧
延使用特性の劣化を有効に防止できると考えるに
到つた。 本発明はかかる独自の技術的見地に基づき、鋳
造のままで外殻高クロム材質中に黒鉛を晶出する
複合高クロムロールを提供せんとするものであ
る。すなわち、本発明は上記目的を達成すべく高
クロム鋳鉄の化学成分、組成を改良工夫したもの
であつて、高クロムロールとしてC2.4〜3.4、
Si2.0〜3.4、Mn0.5〜1.5、P0.1以下、S0.08以下、
Ni4.5〜10、Cr5〜10、Mo0.4〜1.5を各重量%含
み、残部実質的にFeからなり、かつ組成中に黒
鉛を晶出している外殻と、高級鋳鉄、ダクタイル
鋳鉄もしくは黒鉛鋳鋼からなる内殻とを溶着一体
化せしめてなることを特徴とするものである。 一般にクロムは炭化物形成に大きく寄与し、炭
素含有量の増加につれて黒鉛の晶出を抑えるため
通常高クロム鋳鉄の基地組織には硬い炭化物のみ
が存在しているが、上記成分組成範囲にある本発
明の複合高クロムロールでは、その組織中に微細
な黒鉛の均一分布が認められる。 本ロールにおける内殻材質については、従来と
同様の各種鋳鉄・鋳鋼材質を用いることができ別
段特色はない。また本ロールの製造方法について
も、上記成分の高クロム鋳鉄を遠心力鋳造した
後、公知の複合化技術により内殻(軸芯材)を溶
着一体化せしめて鋳造することができる。 第1図は本発明に係る複合高クロムロールの構
造一例を概略的に現わし、1は外殻高クロム鋳
鉄、2は各種強靭鋳鉄、鋳鋼からなる内殻(軸芯
材)を示している。 以下本発明に係る外殻高クロム鋳鉄の成分範囲
限定理由について詳述する。 C2.4〜3.4% CはCrと結合してクロムカーバイドを形成す
る他、後述するSi、Niの黒鉛化生成元素により微
細な黒鉛を晶出するものである。しかして、
C2.4%以下ではクロムカーバイドが減少すると
共に黒鉛の晶出もなくなり、目的とする高クロム
鋳鉄が得られなくなるためである。一方C3.4%
以上ではCr含有量との関係によるものが、本発
明の場合ではCr10%以下に抑えられるため、過
飽和の炭素が高いSi、Ni含有量のため黒鉛化し、
黒鉛晶出量が過剰となつて耐摩耗性の点で劣化す
るためである。 Si2.0〜3.4 Siは高クロム材質に黒鉛を晶出させるために必
要で、2.0%以下ではこの効果がなく3.4%以上で
は黒鉛晶出が過多となり耐摩耗性の点で劣化する
ためである。なおSiについては鋳込前のSi量を上
記成分範囲よりも低目にしておいて、鋳込時に接
種を行ない、最終制品の成分で上記範囲内に調整
する方が黒鉛の晶出に有効である。 Mn0.5〜1.5% Mnは溶湯の脱酸のためにSiと共に積極的に添
加される。Mn0.5%以下ではこの効果が不足し、
1.5%以上では機械的性質特に靭性の点で劣化が
著しくなるためである。 P0.1%以下 Pはロール材質においては少ない程望ましく、
材質を脆くするという点から0.1%以下とする。 S0.08%以下 SもPと同様に少ない程望ましく、やはり材質
を脆くすることから0.08%以下とする。 Ni4.5〜10% Niは基地組織の改良と黒鉛晶出の目的で積極
的に含有される。しかしてNi4.5%以下では黒鉛
の晶出がみられず、一方10%以上になるとSiの場
合と同様黒鉛過多となり、同時に残留オーステナ
イトが増加して後の熱処理によつてもオーステナ
イトが安定で使用時に耐肌荒性の面で問題となる
ためである。 Cr5〜10% CrはCと結合してCr炭化物を形成するが、5
%以下では炭化物が少なく耐摩耗性の点で劣り、
一方10%以上では上記Ni、Siの成分範囲によつて
も黒鉛の晶出が得られないためである。 Mo0.4〜1.5% Moは焼入焼戻し抵抗を高めると共に炭化物中
に入り、炭化物硬度を高めると同時に焼戻し軟化
抵抗を向上させるのに有効であるが、その含有量
が0.4%以下ではこのような効果が少なく、一方
1.5%以上では白銑化傾向が強くなつて黒鉛の晶
出が得られなくなるためである。 本発明の、外殻は以上の成分のほか残部実質的
にFeで形成されるが、その材質特性を向上させ
るためにFeに代えて下記のNb、Vを必要に応じ
て含有することができる。 Nb、V1.0%以下 Nb、Vは共に鋳造組織の微細化に効果があ
り、必要に応じ単独又は複合で1.0%以下含有さ
れる。すなわち、それらが合計量で1.0%以上含
まれると、炭素と結びついてVC、NbC、Nb2Cを
形成し黒鉛の晶出を妨げると共にコスト高となる
ためである。 次に本発明の実施例を従来例と共に掲げて説明
する。 製品胴径φ680、胴長1800 l、全長3800 lの
複合高クロムロールを下記の如く製造すると共に
種々の調査に供した。 外殻として第1表に示す化学成分の高クロム
鋳鉄溶湯を用い、これを遠心力鋳造機上で回転
する鋳型に1410℃の鋳込温度で肉厚80mm(鋳込
重量2T400Kg)鋳込んだ。 外殻が完全に凝固した後(鋳込開始から22〜
23分後)、外殻を内有した遠心力鋳造用鋳型を
垂直に立てて、上部から軸芯材として第1表に
示した内殻溶湯を1380℃で鋳込み鋳型内を完全
に満たした後、上端を押湯保温材でカバーし
た。
The present invention relates to a composite high chromium roll having graphite crystallized in a high chromium outer shell material. Metallurgically, high chromium rolls are made up of fine chromium carbides in their base structure.
It is characterized by excellent wear resistance, but on the other hand, it has low thermal conductivity, and when used for hot rolling under the same rolling conditions, the temperature of the outermost surface of the body in contact with the rolled material is lower than that of other rolls with good thermal conductivity. The problem is that the increase is large. This is because the temperature difference on the surface of the roll cylinder adversely affects the roughness resistance, abrasion resistance, and crack resistance of the roll. One way to improve this drawback is to reduce the amount of chromium as much as possible, but carbide decreases in relation to the carbon content, making it impossible to maintain the excellent wear resistance inherent to high chromium rolls. Therefore, there is a limit. By the way, the conventional technical wisdom is that high chromium rolls have only hard carbides in their structure and no graphite crystallizes at all, and in fact, no rolls containing graphite have ever been found. According to the inventor's research, if it is possible to crystallize graphite in its composition, it is possible to improve the thermal conductivity of high chromium rolls, thereby effectively counteracting the deterioration of the rolling use characteristics mentioned above. I have come to think that it can be prevented. Based on this unique technical viewpoint, the present invention aims to provide a composite high chromium roll in which graphite is crystallized in the high chromium outer shell material as cast. That is, the present invention improves the chemical composition and composition of high chromium cast iron in order to achieve the above object.
Si2.0~3.4, Mn0.5~1.5, P0.1 or less, S0.08 or less,
An outer shell containing 4.5 to 10% Ni, 5 to 10 Cr, and 0.4 to 1.5% by weight, with the remainder essentially consisting of Fe and crystallized graphite in the composition, and high-grade cast iron, ductile cast iron, or graphite. It is characterized by being integrally welded with an inner shell made of cast steel. In general, chromium greatly contributes to the formation of carbides, and as the carbon content increases, the crystallization of graphite is suppressed. Therefore, normally only hard carbides exist in the matrix structure of high chromium cast iron, but the present invention, which has a composition within the above range. In the composite high chromium roll, a uniform distribution of fine graphite is observed in its structure. As for the inner shell material of this roll, the same various cast iron and cast steel materials as conventional ones can be used, and there is no special feature. Also, regarding the manufacturing method of this roll, after centrifugally casting high chromium cast iron having the above components, the inner shell (shaft core material) can be integrally welded and cast using a known composite technology. FIG. 1 schematically shows an example of the structure of a composite high chromium roll according to the present invention, and 1 shows an outer shell of high chromium cast iron, and 2 shows an inner shell (core material) made of various types of tough cast iron and cast steel. . The reason for limiting the range of components of the high chromium cast iron shell according to the present invention will be explained in detail below. C2.4 to 3.4% C combines with Cr to form chromium carbide, and also crystallizes fine graphite with the graphitization forming elements of Si and Ni, which will be described later. However,
This is because if C2.4% or less, chromium carbide decreases and graphite crystallization also stops, making it impossible to obtain the desired high-chromium cast iron. On the other hand, C3.4%
The above is due to the relationship with the Cr content, but in the case of the present invention, since Cr is suppressed to 10% or less, supersaturated carbon graphitizes due to the high Si and Ni contents.
This is because the amount of graphite crystallized becomes excessive and the wear resistance deteriorates. Si2.0 to 3.4 Si is necessary to crystallize graphite in high-chromium materials, and if it is less than 2.0%, this effect will not occur, and if it is more than 3.4%, graphite crystallization will be excessive and the wear resistance will deteriorate. . Regarding Si, it is more effective to crystallize graphite if the amount of Si before casting is lower than the above composition range, inoculated at the time of casting, and the composition of the final product is adjusted within the above range. be. Mn0.5-1.5% Mn is actively added together with Si to deoxidize the molten metal. This effect is insufficient when Mn is less than 0.5%,
This is because if the content exceeds 1.5%, the mechanical properties, especially the toughness, will deteriorate significantly. P0.1% or less The smaller the P content in the roll material, the more desirable it is.
The content should be 0.1% or less in order to make the material brittle. S: 0.08% or less Like P, the lower the S content, the more desirable it is, and since it also makes the material brittle, it should be kept at 0.08% or less. Ni4.5-10% Ni is actively included for the purpose of improving the matrix structure and crystallizing graphite. However, if Ni is less than 4.5%, no crystallization of graphite is observed, while if it is more than 10%, there will be an excessive amount of graphite as in the case of Si, and at the same time, retained austenite will increase and the austenite will not be stable even during subsequent heat treatment. This is because it poses a problem in terms of roughness resistance during use. Cr5~10% Cr combines with C to form Cr carbide, but 5%
% or less, there are few carbides and the wear resistance is poor.
On the other hand, if the content exceeds 10%, crystallization of graphite cannot be obtained even in the above-mentioned ranges of Ni and Si components. Mo0.4-1.5% Mo increases the quenching and tempering resistance and enters into the carbide, and is effective in increasing the hardness of the carbide and simultaneously improving the tempering and softening resistance. However, if its content is below 0.4%, such less effective, while
This is because if it exceeds 1.5%, the tendency to white iron becomes strong and graphite crystallization cannot be obtained. In addition to the above-mentioned components, the outer shell of the present invention is substantially made of Fe; however, in place of Fe, the following Nb and V can be contained as necessary in order to improve the material properties. . Nb, V 1.0% or less Nb and V are both effective in refining the casting structure, and may be contained alone or in combination at 1.0% or less as necessary. That is, if they are contained in a total amount of 1.0% or more, they combine with carbon to form VC, NbC, and Nb 2 C, which impede crystallization of graphite and increase costs. Next, embodiments of the present invention will be described together with conventional examples. A composite high chromium roll having a body diameter of φ680, a body length of 1800 liters, and a total length of 3800 liters was manufactured as described below and subjected to various investigations. A high chromium cast iron molten metal having the chemical composition shown in Table 1 was used as the outer shell, and this was cast into a mold rotating on a centrifugal casting machine at a casting temperature of 1410°C to a wall thickness of 80 mm (casting weight 2T400Kg). After the outer shell has completely solidified (22~
After 23 minutes), the centrifugal casting mold with the outer shell inside was set vertically, and the inner shell molten metal shown in Table 1 was poured from the top as the shaft core material at 1380℃, and the inside of the mold was completely filled. , the upper end was covered with a riser heat insulator.

【表】【table】

【表】 完全に冷却した後、ロールを鋳型から取り出
し、歪取り熱処理(500℃×10Hr)及び組織安
定化熱処理(550℃×15Hr)を行なつた。 このようにして製造されたロールの製品組成
を第2表に示す。また、ロールの胴部について
超音波探傷を行なつた結果、外殻と内殻とは完
全に結合しているのが確認された。更に、実施
例1の外殻について顕微鏡組織観察した結果を
第2図に示す。第2図より明らかな通り、所期
目的とする微細な黒鉛、クロムカーバイド及び
基地からなる組織が得られていることが確認さ
れた。 外殻硬度及び内殻強度を調べた結果を第3表
に示す。
[Table] After completely cooling, the roll was taken out from the mold and subjected to strain relief heat treatment (500°C x 10 hours) and structure stabilization heat treatment (550°C x 15 hours). The product composition of the roll thus produced is shown in Table 2. Further, as a result of ultrasonic flaw detection performed on the body of the roll, it was confirmed that the outer shell and inner shell were completely connected. Furthermore, the results of microstructural observation of the outer shell of Example 1 are shown in FIG. As is clear from FIG. 2, it was confirmed that the desired structure consisting of fine graphite, chromium carbide, and matrix was obtained. Table 3 shows the results of examining the outer shell hardness and inner shell strength.

【表】 次に外殻材について、フアビリー試験により
耐焼付性を調べた。 (i) フアビリー試験は、第3図に示すように、
テストピン11の一端を回転機12にシアー
ピン13によつて固定し、その他端を一定荷
重Pの下で一対のVブロツク14,14によ
り挾み付けながらテストピン11を回転さ
せ、回転に要したトルクにより焼付の有無、
程度を調べるものである。 (ii) フアビリー試験の試験条件は下記の通りで
あつた。 テストピン寸法……φ6.5×40 l Vブロツク寸法……φ12 テストピン回転数……300rpm(0.1m/sec) 負荷荷重P……35Kg 試験環境……無潤滑 (iii) フアビリー試験の結果を第4図及び第5図
に示す。第4図は実施例2、第5図は従来例
に対応したものである。 尚、黒鉛の晶出のない下記成分の比較材に
ついても試験され、その結果を第6図に示
す。 比較材化学組成(重量%) C:2.86% Si:0.92% Mn:0.60% P:0.072% S:0.013% Ni:7.40% Cr:8.29% Mo:0.73% 残部実質的Fe (iv) 第4図より本発明に係る外殻材について
は、トルクの上昇がほとんど認められず焼付
き現象が生じなかつたことが判る。 一方、従来の高クロム材である従来例の外
殻材については、第5図より12秒後に焼付が
生じ始め爾後強固に焼付が生じていることが
判る。また、実施例1の外殻材とSiを除きほ
ぼ同様の成分である比較材についても、第6
図より9〜10秒後でトルクが急激に上がり19
秒で最大になつており、焼付の発生が看取さ
れる。 実施例2、従来例の外殻材及びの比較材に
ついて600℃における熱伝導率を調べた。その
結果を下記に示す。 熱伝導率Cal/cm.seo.℃ 実施例2 5.3×10-2 従来例 5.4×10-2 比較材 4.7×10-2 上記結果から、本発明外殻材の熱伝導率は、従
来材とほとんど変らなかつたが、成分がほぼ同様
の比較材に対しては大幅な向上が認められた。 熱伝導率が従来材とほとんど変らなかつたの
は、黒鉛の有無よりも成分の相違が大きかつたた
めと考えられる。尤も、硬度測定の結果及び耐焼
付性の試験結果から、本発明の外殻は従来の高ク
ロム材に対して、耐摩耗性及び特に耐焼付性に優
れており、延いてはこれらの総合的結果として耐
肌荒性にも優れることが明らかであり、また黒鉛
の生成によりクラツクの進展を有効に阻止できる
ため、耐クラツク性にも優れることが明らかとな
つた。 以上説明した通り、本発明の外殻は、Ni含有
量の多いクロム材質中に鋳造のままで微細な黒鉛
が晶出したものであるから、耐摩耗性、耐クラツ
ク性及び特に耐焼付性が優れたものとなり、延い
ては耐肌荒性の向上にも大きく寄与することがで
きた。また、本発明の内殻は、外殻中のCr含有
量が比較的少ないため外殻から内殻へのCrの混
入、拡散を軽減することができ、内殻の強靭性を
向上させることができた。
[Table] Next, the seizure resistance of the outer shell material was investigated by a fabrication test. (i) As shown in Figure 3, the fabilly test
One end of the test pin 11 is fixed to the rotating machine 12 with a shear pin 13, and the test pin 11 is rotated while the other end is held between a pair of V blocks 14 and 14 under a constant load P. The presence or absence of seizure depending on the torque,
This is to check the degree. (ii) The test conditions for the fabilly test were as follows. Test pin dimensions...φ6.5×40l V block dimensions...φ12 Test pin rotation speed...300rpm (0.1m/sec) Applied load P...35Kg Test environment...no lubrication (iii) Results of the fabilly test It is shown in FIGS. 4 and 5. FIG. 4 corresponds to the second embodiment, and FIG. 5 corresponds to the conventional example. A comparative material with the following components without crystallization of graphite was also tested, and the results are shown in FIG. Comparative material chemical composition (wt%) C: 2.86% Si: 0.92% Mn: 0.60% P: 0.072% S: 0.013% Ni: 7.40% Cr: 8.29% Mo: 0.73% Balance substantial Fe (iv) Figure 4 It can be seen that with the outer shell material according to the present invention, almost no increase in torque was observed and no seizure phenomenon occurred. On the other hand, with respect to the conventional shell material, which is a conventional high-chromium material, it can be seen from FIG. 5 that seizure began to occur after 12 seconds, and the seizure continued to occur strongly thereafter. Also, regarding the comparative material, which has almost the same components as the outer shell material of Example 1 except for Si, the sixth
Torque increases rapidly after 9 to 10 seconds as shown in the figure19
It reaches its maximum within seconds, indicating that burn-in has occurred. The thermal conductivity at 600°C was investigated for the shell material of Example 2, the conventional example, and the comparative material. The results are shown below. Thermal conductivity Cal/cm.seo.℃ Example 2 5.3×10 -2 Conventional example 5.4×10 -2 Comparative material 4.7×10 -2 From the above results, the thermal conductivity of the outer shell material of the present invention is equal to that of the conventional material. Although there was almost no change, a significant improvement was observed compared to the comparative material, which had almost the same composition. The reason why the thermal conductivity was almost the same as that of conventional materials is thought to be because the difference in components was greater than the presence or absence of graphite. However, from the hardness measurement results and seizure resistance test results, the outer shell of the present invention has superior wear resistance and especially seizure resistance compared to conventional high chromium materials, and furthermore, the overall As a result, it is clear that it has excellent roughening resistance, and it has also become clear that it has excellent crack resistance because the growth of cracks can be effectively inhibited by the formation of graphite. As explained above, the outer shell of the present invention has fine graphite crystallized in a chromium material with a high Ni content as it is cast, so it has excellent wear resistance, crack resistance, and especially seizure resistance. This resulted in excellent results, which in turn made a significant contribution to improving the roughness resistance. In addition, since the inner shell of the present invention has a relatively low Cr content in the outer shell, it is possible to reduce the mixing and diffusion of Cr from the outer shell to the inner shell, and improve the toughness of the inner shell. did it.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明に係る複合高クロムロールの構
造例を概略的に現わす断面図である。第2図は本
発明の実施例ロールについての外殻組織を現わす
顕微鏡写真(倍率50倍)、第3図はフアビリー試
験要領説明図、第4図〜第5図はフアビリー試験
結果を示すグラフ図であり、第4図は実施例外殻
材、第5図は従来例外殻材、第6図は比較材に係
るものである。 1……外殻、2……内殻(軸芯材)。
FIG. 1 is a sectional view schematically showing a structural example of a composite high chromium roll according to the present invention. Fig. 2 is a micrograph (50x magnification) showing the outer shell structure of an example roll of the present invention, Fig. 3 is an explanatory diagram of the fuabilly test procedure, and Figs. 4 and 5 are graphs showing the fuabilly test results. FIG. 4 shows an example shell material, FIG. 5 shows a conventional shell material, and FIG. 6 shows a comparative material. 1... Outer shell, 2... Inner shell (shaft core material).

Claims (1)

【特許請求の範囲】[Claims] 1 C2.4〜3.4、Si2.0〜3.4、Mn0.5〜1.5、P0.1以
下、S0.08以下、Ni4.5〜10、Cr5〜10、Mo0.4〜
1.5を各重量%含み、残部実質的にFeからなり、
かつ組織中に黒鉛を晶出している外殻と、高級鋳
鉄、ダクタイル鋳鉄もしくは黒鉛鋳鉄からなる内
殻とを溶着一体化せしめてなることを特徴とする
黒鉛を有する高クロムロール。
1 C2.4~3.4, Si2.0~3.4, Mn0.5~1.5, P0.1 or less, S0.08 or less, Ni4.5~10, Cr5~10, Mo0.4~
1.5% by weight, the remainder substantially consists of Fe,
A high chromium roll containing graphite, characterized in that an outer shell in which graphite is crystallized in its structure and an inner shell made of high-grade cast iron, ductile cast iron, or graphite cast iron are welded and integrated.
JP7394782A 1982-04-30 1982-04-30 High chromium roll containing graphite Granted JPS58193343A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7394782A JPS58193343A (en) 1982-04-30 1982-04-30 High chromium roll containing graphite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7394782A JPS58193343A (en) 1982-04-30 1982-04-30 High chromium roll containing graphite

Publications (2)

Publication Number Publication Date
JPS58193343A JPS58193343A (en) 1983-11-11
JPS6116415B2 true JPS6116415B2 (en) 1986-04-30

Family

ID=13532793

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7394782A Granted JPS58193343A (en) 1982-04-30 1982-04-30 High chromium roll containing graphite

Country Status (1)

Country Link
JP (1) JPS58193343A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60124407A (en) * 1983-12-06 1985-07-03 Kubota Ltd High vanadium composite cast iron roll
JPS61557A (en) * 1984-06-13 1986-01-06 Kubota Ltd Hot run table roller
JPH07103443B2 (en) * 1987-04-15 1995-11-08 株式会社クボタ High hardness graphite crystallized high chromium material with excellent wear resistance and composite roll for rolling
JP2542681B2 (en) * 1988-07-19 1996-10-09 日立金属株式会社 Wear-resistant alloy cast iron
JPH0293040A (en) * 1988-09-29 1990-04-03 Kubota Ltd Graphite-crystallized high-chrome cast iron roll material having excellent seizure resistance and wear resistance
US5202087A (en) * 1992-07-31 1993-04-13 The Carondelet Corporation Cement cooler grate alloy

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55158250A (en) * 1979-05-28 1980-12-09 Kubota Ltd High-hardness high-chromium roll

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55158250A (en) * 1979-05-28 1980-12-09 Kubota Ltd High-hardness high-chromium roll

Also Published As

Publication number Publication date
JPS58193343A (en) 1983-11-11

Similar Documents

Publication Publication Date Title
JPS6116415B2 (en)
JPS6014095B2 (en) Alloy chilled roll material with excellent crack resistance and wear resistance
JP3343538B2 (en) Rolling roll
JP2635973B2 (en) High hardness graphite crystallized high chromium composite roll
JPH0692625B2 (en) Roll for hot rolling
JPS6320627B2 (en)
JPH0823060B2 (en) High chromium composite roll with graphite
JP3056703B2 (en) Rolling roll outer layer material and rolling roll using the same
JPH0227431B2 (en) KOKUENOJUSURUKOKUROMUROORU
JPS6333543A (en) Graphite-crystallized high-chromium roll material
JPS61199051A (en) Roll material for rolling excellent in heat cracking resistance, wear resistance and seizure resistance
JPS5810982B2 (en) High hardness chrome roll for cold rolling
JPS6116336B2 (en)
JP2672598B2 (en) Graphite-crystallized high chromium cast iron roll material and composite roll for rolling with excellent wear resistance and surface roughness
JP2795557B2 (en) Composite roll
JPH0293039A (en) Graphite-crystallized high-chrome cast iron roll material having excellent seizure resistance and wear resistance
JPS60121013A (en) Composite roll for strip mill
JP3219987B2 (en) Graphite crystallized high-speed cast iron material with excellent skin resistance
JPH0353043A (en) High chromium cast iron roll stock excellent in cracking resistance and slip resistance
JPH03281753A (en) High alloy cast iron material having excellent resistance to roughening of surface
JP2636020B2 (en) Graphite-crystallized high chromium cast iron roll material and composite roll for rolling with excellent wear resistance and surface roughness
JPS6363507A (en) Tough roll
JPH02290942A (en) High chromium cast iron roll material having excellent crack resistance, slip resistance and seizure resistance
JPH09263873A (en) High speed steel type cast iron material containing crystallized graphite, excellent in wear resistance
JPH0313542A (en) Graphite crystallized high molybdenum cast iron material having excellent wear resistance